Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Apex Arc Hip Stem Recalled by Omnilife Science Inc. Due to Staining on hip implant.

Date: May 9, 2014
Company: Omnilife Science Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Omnilife Science Inc. directly.

Affected Products

Apex Arc Hip Stem, Size 2, HA Coated; Product Code: HC-21002-HA

Quantity: 13 devices

Why Was This Recalled?

Staining on hip implant.

Where Was This Sold?

This product was distributed to 7 states: CA, FL, MA, NY, OK, TX, VA

Affected (7 states)Not affected

About Omnilife Science Inc.

Omnilife Science Inc. has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report